Suzanne Walton
University College London
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BMJ Open Respiratory Research | 2018
Lucy J Griffiths; Ronan Lyons; Amrita Bandyopadhyay; Karen Tingay; Suzanne Walton; Mario Cortina-Borja; Ashley Akbari; Helen Bedford; Carol Dezateux
Introduction Electronic health records (EHRs) are increasingly used to estimate the prevalence of childhood asthma. The relation of these estimates to those obtained from parent-reported wheezing suggestive of asthma is unclear. We hypothesised that parent-reported wheezing would be more prevalent than general practitioner (GP)-recorded asthma diagnoses in preschool-aged children. Methods 1529 of 1840 (83%) Millennium Cohort Study children registered with GPs in the Welsh Secure Anonymised Information Linkage databank were linked. Prevalences of parent-reported wheezing and GP-recorded asthma diagnoses in the previous 12 months were estimated, respectively, from parent report at ages 3, 5, 7 and 11 years, and from Read codes for asthma diagnoses and prescriptions based on GP EHRs over the same time period. Prevalences were weighted to account for clustered survey design and non-response. Cohen’s kappa statistics were used to assess agreement. Results Parent-reported wheezing was more prevalent than GP-recorded asthma diagnoses at 3 and 5 years. Both diminished with age: by age 11, prevalences of parent-reported wheezing and GP-recorded asthma diagnosis were 12.9% (95% CI 10.6 to 15.4) and 10.9% (8.8 to 13.3), respectively (difference: 2% (−0.5 to 4.5)). Other GP-recorded respiratory diagnoses accounted for 45.7% (95% CI 37.7 to 53.9) and 44.8% (33.9 to 56.2) of the excess in parent-reported wheezing at ages 3 and 5 years, respectively. Conclusion Parent-reported wheezing is more prevalent than GP-recorded asthma diagnoses in the preschool years, and this difference diminishes in primary school-aged children. Further research is needed to evaluate the implications of these differences for the characterisation of longitudinal childhood asthma phenotypes from EHRs.
Vaccine | 2017
Suzanne Walton; Mario Cortina-Borja; Carol Dezateux; Lucy J Griffiths; Karen Tingay; Ashley Akbari; Amrita Bandyopadhyay; Ronan Lyons; Helen Bedford
Highlights • Most children received the first dose of primary vaccines on time.• Timeliness of vaccination decreased with vaccine dose.• Most children had appropriate intervals between doses; marked variation occurred.• The quality of routine vaccination records in Wales is high.• Parental report of MMR status is reliable.
The Lancet | 2013
Carol Dezateux; Peter Brocklehurst; Simon Burgess; Paul R. Burton; Anne Carey; Debbie Colson; Chris Dibben; Paul Elliott; Alan Emond; Harvey Goldstein; Hilary Graham; Frank J. Kelly; Rachel L Knowles; David A. Leon; Ronan Lyons; Diane Reay; Anna Vignoles; Suzanne Walton
Abstract Background Health and social policies relevant to improving the lives of children draw on understanding of early life developmental trajectories and the social and material environments in which children are born and grow up. These policies draw on information from the UKs unique birth cohorts (comprising cohorts from 1946, 1958, 1970, and 2000 that have been assessed repeatedly to the present day) and other longitudinal studies. The importance of intergenerational and intragenerational effects on child health and development in the UK is increasingly recognised. A cross-disciplinary approach to the lifecourse is needed to meet this pressing scientific public health and policy challenge, which is sensitive to social, gender, and ethnic inequalities and incorporates biomedical, clinical, and social sciences from the outset. We will create a longitudinal data resource to address questions and hypotheses relevant to improving the lives of children, both now and in their futures. Five major research themes will be explored: inequalities, diversity, and social mobility; early life antecedents of school readiness and later educational performance; developmental origins of health and ill-health in childhood; social, emotional, and behavioural development: the interplay between infant and parent; and neighbourhoods and environment: effects on child and family. Methods A multidisciplinary scientific leadership team is responsible for the detailed scientific design and protocol. Methods used to support protocol development and delivery include systematic review; process models; consultation with academics, policy makers, and parents; development of an ethics and governance framework; data simulations; and power calculations. The study has been designed to provide sufficient statistical power to address key scientific hypotheses and to provide nationally representative statistical information. It consists of two components: mothers and partners recruited during pregnancy through selected maternity units and those recruited after birth through probability-based sampling of the birth register. These sampling methods allow the larger component of pregnant mothers to be geographically clustered and ethnically diverse while increasing the precision of estimates for nationally representative measures. Mothers will be invited to attend a Life Study centre local to their maternity unit once during pregnancy and twice during the first year of life; fathers or partners will also be seen antenatally. Biological samples will be taken at the visits and at birth. Parents and babies in the probability sample will be contacted twice in the first year. Up to 90 000 children will be recruited with whom contact will be maintained through childhood and into adult life. An achieved sample size of 50 000 by 12 months would provide adequate power to detect moderately strong causal effects of risk factors (environmental, psychosocial, genetic) that are moderately common (eg, prevalence ≥10%) on outcomes of public health importance (eg, prevalence ≥2%, including asthma, obesity, autism spectrum disorders, and learning difficulties). Ethics and information governance approvals have been obtained and an ethics framework developed. Data enhancements that are under development address infection and immunity, the role of fathers or partners, and home-based environmental exposures. Interpretation Life Study offers an opportunity to develop and test our understanding of social and biological mechanisms operating through the lifecourse and to identify translational opportunities for policy and practice relevant to childrens lives. Funding Life Study is supported by the Economic and Social Research Council, the Medical Research Council, and University College London. It is part of the Birth Cohort Facility Project, which receives funding from the governments Large Facilities Capital Fund.
BMJ | 2006
Suzanne Walton; Helen Bedford; Carol Dezateux
Archives of Disease in Childhood | 2007
Suzanne Walton; David Elliman; Helen Bedford
In: Children of the 21st Century: From Birth to Nine Months. (pp. 133-158). (2005) | 2005
Carol Dezateux; L Foster; Tate Ar; Suzanne Walton; Samad L; Helen Bedford
International Journal for Population Data Science | 2018
Amrita Bandyopadhyay; Karen Tingay; Ashley Akbari; Lucy J Griffiths; Mario Cortina-Borja; Helen Bedford; Suzanne Walton; Carol Dezateux; Ronan Lyons
International Journal for Population Data Science | 2018
Amrita Bandyopadhyay; Karen Tingay; Mario Cortina Borja; Lucy J Griffiths; Ashley Akbari; Helen Bedford; Sinead Brophy; Suzanne Walton; Carol Dezateux; Ronan Lyons
Longitudinal and life course studies | 2017
Suzanne Walton; Stelios Alexandrakis; Nicholas Gilby; Nicola Firman; Gareth Williams; Duncan Peskett; Peter Elias; Carol Dezateux
International Journal for Population Data Science | 2017
Karen Tingay; Ashley Akbari; Amrita Bandyopadhyay; Helen Bedford; Sinead Brophy; Mario Cortina Borja; Emla Fitzsimons; Lucy J Griffiths; Melanie A. Healy; Jon Johnson; Efrosini Setakis; Suzanne Walton; Carol Dezateux; Ronan Lyons